ArticleAnnals of medicine2026
Development and validation of a nomogram to predict 28-day all-cause mortality in sepsis patients complicated by acute kidney injury.
Article in Annals of medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundSepsis-induced acute kidney injury (SAKI) carries substantial morbidity and mortality, yet prognostic factors for 28-day all-cause mortality remain inadequately characterized. This study aimed to develop and validate a nomogram for predicting 28-day all-cause mortality in SAKI patients.
methodsThis single-center retrospective cohort study enrolled 857 consecutive SAKI patients from the Affiliated Hospital of Southwest Medical University (December 2018-June 2025), randomly divided into training (n=601, 70%) and internal validation (n=256, 30%) sets. Candidate predictors were initially identified using LASSO regression coupled with ten-fold cross-validation to tune the optimal lambda parameter. Variables possessing non-zero coefficients in the LASSO model were subsequently incorporated into multivariate logistic regression employing backward stepwise elimination to ascertain independent risk factors for 28-day all-cause mortality. A predictive nomogram was then constructed, and model performance was assessed using receiver operating characteristic (ROC), calibration, and decision curve analysis (DCA).
resultsLASSO regression identified 11 predictors of 28-day mortality in the training set. Subsequent multivariate logistic regression demonstrated that age, hospital stay (the actual length at the time of SAKI diagnosis), respiratory failure, heart failure, hepatic failure, APTT and mechanical ventilation were independent predictors of 28-day all-cause mortality. The 7-variable nomogram yielded area under the curves (AUCs) of 0.854 and 0.795 in the training and validation cohorts, respectively. Calibration metrics revealed a slope of 1.000 and Brier score of 0.142 in the training set, compared with 0.762 and 0.173 in the validation set. Decision curve analysis (DCA) substantiated the advantageous clinical applicability of the prognostic model.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.